NDC 66077-773 Instant Foam

  1. Labeler Index
  2. Ultra-chem Inc.
  3. NDC: 66077-773 Instant Foam

NDC Product Code 66077-773

NDC CODE: 66077-773

Proprietary Name: Instant Foam What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

NDC 66077-773-25

Package Description: 199 g in 1 CAN

NDC 66077-773-26

Package Description: 454 g in 1 CAN

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Instant Foam with NDC 66077-773 is a product labeled by Ultra-chem Inc.. The generic name of Instant Foam is . The product's dosage form is and is administered via form.

Labeler Name: Ultra-chem Inc.

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.
  • PROPANE (UNII: T75W9911L6)
  • BUTANE (UNII: 6LV4FOR43R)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Ultra-chem Inc.
Labeler Code: 66077
Start Marketing Date: 03-01-2010 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2017 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag: I What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Instant Foam Product Label Images

Instant Foam Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Drug Facts Box Otc-Active Ingredients Section

Ethyl Alcohol 62%

Drug Facts Box Otc-Purpose Section

Antiseptic

Drug Facts Box Otc-Indications And Usage Section

For hand-washing to decrease bacteria on the skin, only when water is not available

Drug Facts Box Otc-Warnings Section

Flammable, keep away from fire and flamesFor external use only

Drug Facts Box Otc-When Using Section

Do not get into eyesif contact occurs, rinse eyes thoroughly with water

Drug Facts Box Otc-Stop Use Section

Irritation and redness develop

Drug Facts Box Otc-Keep Out Of Reach Of Children Section

If swallowed, get medical help or contact a Poison Control Center right away

Drug Facts Box Otc-Dosage & Administration Section

Press valve once to deliver one squirt (about a quarter size) of foaming product onto the palm of your handrub hands together and allow to dry without wiping

Drug Facts Box Otc-Inactive Ingredients Section

Water, DEA-C8-18 perfluoroalkylethyl phosphate, cetearyl alcohol, polysorbate 65, dimethicone PEG-8 meadowfoamate, meadowfoamamidopropyl betaine, butane, propane, fragrance

Instant Foam 4773 199G

477307F4150.jpg Instant Foam 199g

* Please review the disclaimer below.